![]() 1,3-Bis[3,5-bis(trifluoromethyl)phenyl]thiourea structure
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Common Name | 1,3-Bis[3,5-bis(trifluoromethyl)phenyl]thiourea | ||
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CAS Number | 1060-92-0 | Molecular Weight | 500.30500 | |
Density | 1.604g/cm3 | Boiling Point | 332.7ºC at 760 mmHg | |
Molecular Formula | C17H8F12N2S | Melting Point | 152 °C | |
MSDS | Chinese USA | Flash Point | 155ºC | |
Symbol |
![]() GHS07 |
Signal Word | Warning |
Name | 1,3-Bis[3,5-bis(trifluoromethyl)phenyl]thiourea |
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Synonym | More Synonyms |
Density | 1.604g/cm3 |
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Boiling Point | 332.7ºC at 760 mmHg |
Melting Point | 152 °C |
Molecular Formula | C17H8F12N2S |
Molecular Weight | 500.30500 |
Flash Point | 155ºC |
Exact Mass | 500.02200 |
PSA | 63.19000 |
LogP | 7.86420 |
Vapour Pressure | 0.000143mmHg at 25°C |
Index of Refraction | 1.503 |
Symbol |
![]() GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319 |
Precautionary Statements | P280-P305 + P351 + P338-P337 + P313 |
RIDADR | NONH for all modes of transport |
Activation of a carbonyl compound by halogen bonding.
Chem. Commun. (Camb.) 50(47) , 6281-4, (2014) Using a prototypical Diels-Alder reaction as benchmark, we show that dicationic halogen-bond donors are capable of activating a neutral organic substrate. By various comparison experiments, the action... |
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Trisubstituted 2-trifluoromethyl pyrrolidines via catalytic asymmetric Michael addition/reductive cyclization.
Org. Lett. 16(9) , 2362-5, (2014) The stereoselective synthesis of trisubstituted 2-trifluoromethyl pyrrolidines by asymmetric Michael addition/hydrogenative cyclization is described. The direct organocatalytic addition of 1,1,1-trifl... |
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Water-compatible hydrogen-bond activation: a scalable and organocatalytic model for the stereoselective multicomponent aza-Henry reaction.
Chemistry 19(49) , 16550-4, (2013)
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1,3-Bis[3,5-bis(trifluoroMethyl)phenyl]thiourea |
1,3-bis[3,5-bis(trifluoromethyl)phenyl]thiourea |